Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Diacap(R) Ultra Dialysis Fluid Filter Recalled by B. Braun Medical, Inc. Due to There is the potential of the residual moisture...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact B. Braun Medical, Inc. directly.
Affected Products
Diacap(R) Ultra Dialysis Fluid Filter, Catalog Number 7107367. Intended to filter bacteria and endotoxins from dialysis fluid.
Quantity: 1580
Why Was This Recalled?
There is the potential of the residual moisture of the Diacap Ultra membrane being reduced over time, which results in the reduction of the membrane permeability (ultrafiltration coefficient).
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About B. Braun Medical, Inc.
B. Braun Medical, Inc. has 216 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report